首页> 美国卫生研究院文献>The Journal of Biological Chemistry >The C-terminal region of A-kinase anchor protein 350 (AKAP350A) enables formation of microtubule-nucleation centers and interacts with pericentriolar proteins
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The C-terminal region of A-kinase anchor protein 350 (AKAP350A) enables formation of microtubule-nucleation centers and interacts with pericentriolar proteins

机译:A激酶锚蛋白350(AKAP350A)的C端区域能够形成微管成核中心并与中心小周蛋白相互作用

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摘要

Microtubules in animal cells assemble (nucleate) from both the centrosome and the cis-Golgi cisternae. A-kinase anchor protein 350 kDa (AKAP350A, also called AKAP450/CG-NAP/AKAP9) is a large scaffolding protein located at both the centrosome and Golgi apparatus. Previous findings have suggested that AKAP350 is important for microtubule dynamics at both locations, but how this scaffolding protein assembles microtubule nucleation machinery is unclear. Here, we found that overexpression of the C-terminal third of AKAP350A, enhanced GFP-AKAP350A(2691–3907), induces the formation of multiple microtubule-nucleation centers (MTNCs). Nevertheless, these induced MTNCs lacked “true” centriole proteins, such as Cep135. Mapping analysis with AKAP350A truncations demonstrated that AKAP350A contains discrete regions responsible for promoting or inhibiting the formation of multiple MTNCs. Moreover, GFP-AKAP350A(2691–3907) recruited several pericentriolar proteins to MTNCs, including γ-tubulin, pericentrin, Cep68, Cep170, and Cdk5RAP2. Proteomic analysis indicated that Cdk5RAP2 and Cep170 both interact with the microtubule nucleation-promoting region of AKAP350A, whereas Cep68 interacts with the distal C-terminal AKAP350A region. Yeast two-hybrid assays established a direct interaction of Cep170 with AKAP350A. Super-resolution and deconvolution microscopy analyses were performed to define the association of AKAP350A with centrosomes, and these studies disclosed that AKAP350A spans the bridge between centrioles, co-localizing with rootletin and Cep68 in the linker region. siRNA-mediated depletion of AKAP350A caused displacement of both Cep68 and Cep170 from the centrosome. These results suggest that AKAP350A acts as a scaffold for factors involved in microtubule nucleation at the centrosome and coordinates the assembly of protein complexes associating with the intercentriolar bridge.
机译:动物细胞中的微管从中心体和顺式高尔基池中组装(成核)。 A激酶锚蛋白350 kDa(AKAP350A,也称为AKAP450 / CG-NAP / AKAP9)是位于中心体和高尔基体的大型支架蛋白。先前的发现表明AKAP350对于两个位置的微管动力学都很重要,但是尚不清楚这种支架蛋白如何组装微管成核机制。在这里,我们发现AKAP350A C末端三分之一的过度表达,即增强的GFP-AKAP350A(2691-3907),诱导了多个微管成核中心(MTNC)的形成。然而,这些诱导的MTNC缺乏“真正的”中心蛋白,例如Cep135。用AKAP350A截短图进行的分析表明,AKAP350A包含负责促进或抑制多个MTNC形成的离散区域。此外,GFP-AKAP350A(2691-3907)向MTNC募集了几种中心粒蛋白,包括γ-微管蛋白,peritcentrin,Cep68,Cep170和Cdk5RAP2。蛋白质组学分析表明Cdk5RAP2和Cep170都与AKAP350A的微管成核促进区域相互作用,而Cep68与远端C端AKAP350A区域相互作用。酵母两杂交试验建立了Cep170与AKAP350A的直接相互作用。进行了超分辨率和去卷积显微镜分析,以定义AKAP350A与中心体的关联,这些研究表明AKAP350A跨越着中心粒之间的桥梁,在连接区中与rootletin和Cep68共定位。 siRNA介导的AKAP350A耗竭导致Cep68和Cep170都从中心体置换。这些结果表明,AKAP350A充当着中心体微管成核相关因子的支架,并协调了与中心间桥相关的蛋白质复合物的组装。

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